A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114308



Internal ID21297574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:48614873..48617349hg38UCSC Ensembl
Innerchr17:46692235..46694711hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg382477
hg192477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv497n145
Supporting Variantsnssv14097646, nssv14098584
Samplessample214, sample361
Known GenesHOXB8
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114308
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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